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ZBTB24 (Zinc Finger and BTB Domain Containing 24) prevents recurrent spontaneous abortion by promoting trophoblast proliferation, differentiation and migration

Recurrent spontaneous abortion (RSA) is a common complication during early gestation, which is associated with aberrant DNA methylation. Zinc Finger and BTB Domain Containing 24 (ZBTB24) plays a critical role in facilitating DNA methylation and cell proliferation. However, the regulatory role of ZBT...

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Autores principales: Ruan, Haibo, Dai, Zhenzhen, Yan, Jinyu, Long, Xiaoxi, Chen, Yi, Yang, Youlin, Yang, Qian, Zhu, Jun, Zheng, Meiyun, Zhang, Xiahui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8973579/
https://www.ncbi.nlm.nih.gov/pubmed/35038951
http://dx.doi.org/10.1080/21655979.2021.2019655
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author Ruan, Haibo
Dai, Zhenzhen
Yan, Jinyu
Long, Xiaoxi
Chen, Yi
Yang, Youlin
Yang, Qian
Zhu, Jun
Zheng, Meiyun
Zhang, Xiahui
author_facet Ruan, Haibo
Dai, Zhenzhen
Yan, Jinyu
Long, Xiaoxi
Chen, Yi
Yang, Youlin
Yang, Qian
Zhu, Jun
Zheng, Meiyun
Zhang, Xiahui
author_sort Ruan, Haibo
collection PubMed
description Recurrent spontaneous abortion (RSA) is a common complication during early gestation, which is associated with aberrant DNA methylation. Zinc Finger and BTB Domain Containing 24 (ZBTB24) plays a critical role in facilitating DNA methylation and cell proliferation. However, the regulatory role of ZBTB24 on trophoblast development in RSA remains unclear. In this study, ZBTB24 expression was compared between decidua tissues of RSA patients and induced abortion controls from a published dataset, which was further validated in placental villi tissues by RT-qPCR and Western blot. The roles of ZBTB24 in trophoblast proliferation, differentiation, and migration were investigated by functional assays after ZBTB24 knockdown or overexpression in HTR-8/SVneo cells. Our results showed that ZBTB24 expression was significantly decreased in RSA patients, and ZBTB24 expression level positively regulated cell viability, differentiation, and migration in HTR-8/SVneo cells. We further demonstrated that ZBTB24 modulated the expression of E-cadherin by altering the DNA methylation at the promoter region. Overall, the downregulation of ZBTB24 is implicated in RSA by inhibiting trophoblast proliferation, differentiation, and migration. Therefore, ZBTB24 may serve as a promising therapeutic target and diagnostic marker for RSA.
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spelling pubmed-89735792022-04-02 ZBTB24 (Zinc Finger and BTB Domain Containing 24) prevents recurrent spontaneous abortion by promoting trophoblast proliferation, differentiation and migration Ruan, Haibo Dai, Zhenzhen Yan, Jinyu Long, Xiaoxi Chen, Yi Yang, Youlin Yang, Qian Zhu, Jun Zheng, Meiyun Zhang, Xiahui Bioengineered Research Paper Recurrent spontaneous abortion (RSA) is a common complication during early gestation, which is associated with aberrant DNA methylation. Zinc Finger and BTB Domain Containing 24 (ZBTB24) plays a critical role in facilitating DNA methylation and cell proliferation. However, the regulatory role of ZBTB24 on trophoblast development in RSA remains unclear. In this study, ZBTB24 expression was compared between decidua tissues of RSA patients and induced abortion controls from a published dataset, which was further validated in placental villi tissues by RT-qPCR and Western blot. The roles of ZBTB24 in trophoblast proliferation, differentiation, and migration were investigated by functional assays after ZBTB24 knockdown or overexpression in HTR-8/SVneo cells. Our results showed that ZBTB24 expression was significantly decreased in RSA patients, and ZBTB24 expression level positively regulated cell viability, differentiation, and migration in HTR-8/SVneo cells. We further demonstrated that ZBTB24 modulated the expression of E-cadherin by altering the DNA methylation at the promoter region. Overall, the downregulation of ZBTB24 is implicated in RSA by inhibiting trophoblast proliferation, differentiation, and migration. Therefore, ZBTB24 may serve as a promising therapeutic target and diagnostic marker for RSA. Taylor & Francis 2022-01-17 /pmc/articles/PMC8973579/ /pubmed/35038951 http://dx.doi.org/10.1080/21655979.2021.2019655 Text en © 2022 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Paper
Ruan, Haibo
Dai, Zhenzhen
Yan, Jinyu
Long, Xiaoxi
Chen, Yi
Yang, Youlin
Yang, Qian
Zhu, Jun
Zheng, Meiyun
Zhang, Xiahui
ZBTB24 (Zinc Finger and BTB Domain Containing 24) prevents recurrent spontaneous abortion by promoting trophoblast proliferation, differentiation and migration
title ZBTB24 (Zinc Finger and BTB Domain Containing 24) prevents recurrent spontaneous abortion by promoting trophoblast proliferation, differentiation and migration
title_full ZBTB24 (Zinc Finger and BTB Domain Containing 24) prevents recurrent spontaneous abortion by promoting trophoblast proliferation, differentiation and migration
title_fullStr ZBTB24 (Zinc Finger and BTB Domain Containing 24) prevents recurrent spontaneous abortion by promoting trophoblast proliferation, differentiation and migration
title_full_unstemmed ZBTB24 (Zinc Finger and BTB Domain Containing 24) prevents recurrent spontaneous abortion by promoting trophoblast proliferation, differentiation and migration
title_short ZBTB24 (Zinc Finger and BTB Domain Containing 24) prevents recurrent spontaneous abortion by promoting trophoblast proliferation, differentiation and migration
title_sort zbtb24 (zinc finger and btb domain containing 24) prevents recurrent spontaneous abortion by promoting trophoblast proliferation, differentiation and migration
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8973579/
https://www.ncbi.nlm.nih.gov/pubmed/35038951
http://dx.doi.org/10.1080/21655979.2021.2019655
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